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SPATA7
5570968.Pdf
Mutation of SPATA7 in a Family with Autosomal Recessive Early-Onset Retinitis Pigmentosa
Screening of SPATA7 in Patients with Leber Congenital Amaurosis and Severe Childhood-Onset Retinal Dystrophy Reveals Disease-Causing Mutations
A Yeast Bifc-Seq Method for Genome-Wide Interactome Mapping
US 2009/0270267 A1 Akiyama Et Al
Content Based Search in Gene Expression Databases and a Meta-Analysis of Host Responses to Infection
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
Comprehensive Genotyping Reveals RPE65 As the Most Frequently Mutated Gene in Leber Congenital Amaurosis in Denmark
Genetics and Retinal Degeneration: Challenges in Optogenetic Therapy and Indentifying Pathogenic Variants
INTRODUCING a NOVEL METHOD for GENETIC ANALYSIS of AUTISM SPECTRUM DISORDER Sepideh Nouri
An Sirna-Based Functional Genomics Screen for the Identification of Regulators of Ciliogenesis and Ciliopathy Genes
ABSTRACT Using a Bioinformatics Approach to Identify Genes That
Part of the SPATA7 Gene in a Consanguineous Israeli Muslim Arab Family
Homozygosity Mapping Reveals Null Mutations in FAM161A As a Cause of Autosomal-Recessive Retinitis Pigmentosa
Mutations in SPATA7 Cause Leber Congenital Amaurosis and Juvenile Retinitis Pigmentosa
Current Concepts of Genotype-Phenotype Correlations
Targeted Sequencing of Linkage Region in Dominican Families
Using Massively Parallel Sequencing to Determine the Genetic Basis of Leigh Syndrome, the Most Common Mitochondrial Disorder Affecting Children
Top View
MRG15 Is Required for Pre-Mrna Splicing and Spermatogenesis
Report 81584
Molecular Genetics of Ocular Diseases
Leber Congenital Amaurosis and Other Autosomal
Genetic Screening of LCA in Belgium: Predominance of CEP290 and Identification of Potential Modifier Alleles in AHI1 of CEP290-R
Molecular Characterisation of Canine Progressive Retinal Atrophies
RNA Sequencing Unravels the Genetics of Refractory/Relapsed T-Cell Acute Lymphoblastic Leukemia
Gene Therapy for Inherited Retinal Disease
Homozygosity Mapping of Consanguineous Families with Leber S Congenital Amaurosis
Mutation Screening of Retinal Dystrophy Patients by Targeted Capture from Tagged Pooled Dnas and Next Generation Sequencing
A Genotype – Phenotype Study of Childhood Onset Retinal